WO2011041729A3 - Compounds as lysophosphatidic acid receptor antagonists - Google Patents
Compounds as lysophosphatidic acid receptor antagonists Download PDFInfo
- Publication number
- WO2011041729A3 WO2011041729A3 PCT/US2010/051199 US2010051199W WO2011041729A3 WO 2011041729 A3 WO2011041729 A3 WO 2011041729A3 US 2010051199 W US2010051199 W US 2010051199W WO 2011041729 A3 WO2011041729 A3 WO 2011041729A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- compounds
- receptor antagonists
- acid receptor
- lysophosphatidic acid
- antagonists
- Prior art date
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/08—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/42—Oxazoles
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/42—Oxazoles
- A61K31/422—Oxazoles not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
- A61K31/4725—Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
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- A—HUMAN NECESSITIES
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D261/14—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D261/18—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
Abstract
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN2177DEN2012 IN2012DN02177A (en) | 2009-10-01 | 2010-10-01 | |
CN201080054528.7A CN102666504B (en) | 2009-10-01 | 2010-10-01 | Compound as lpa receptor antagonist |
EP10821369A EP2483253A4 (en) | 2009-10-01 | 2010-10-01 | Compounds as lysophosphatidic acid receptor antagonists |
JP2012532368A JP2013506695A (en) | 2009-10-01 | 2010-10-01 | Compounds as lysophosphatidic acid receptor antagonists |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US24786109P | 2009-10-01 | 2009-10-01 | |
US61/247,861 | 2009-10-01 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2011041729A2 WO2011041729A2 (en) | 2011-04-07 |
WO2011041729A3 true WO2011041729A3 (en) | 2011-08-04 |
Family
ID=43128102
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2010/051150 WO2011041694A2 (en) | 2009-10-01 | 2010-10-01 | Compounds as lysophosphatidic acid receptor antagonists |
PCT/US2010/051199 WO2011041729A2 (en) | 2009-10-01 | 2010-10-01 | Compounds as lysophosphatidic acid receptor antagonists |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2010/051150 WO2011041694A2 (en) | 2009-10-01 | 2010-10-01 | Compounds as lysophosphatidic acid receptor antagonists |
Country Status (10)
Country | Link |
---|---|
US (3) | US8217066B2 (en) |
EP (2) | EP2483252B1 (en) |
JP (2) | JP2013506694A (en) |
CN (2) | CN102666504B (en) |
AR (1) | AR078497A1 (en) |
GB (1) | GB2474120B (en) |
IN (2) | IN2012DN02177A (en) |
TW (1) | TWI401082B (en) |
UY (1) | UY32926A (en) |
WO (2) | WO2011041694A2 (en) |
Families Citing this family (68)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8455499B2 (en) | 2008-12-11 | 2013-06-04 | Amira Pharmaceuticals, Inc. | Alkyne antagonists of lysophosphatidic acid receptors |
GB2466121B (en) | 2008-12-15 | 2010-12-08 | Amira Pharmaceuticals Inc | Antagonists of lysophosphatidic acid receptors |
GB2470833B (en) | 2009-06-03 | 2011-06-01 | Amira Pharmaceuticals Inc | Polycyclic antagonists of lysophosphatidic acid receptors |
JP2013501064A (en) | 2009-08-04 | 2013-01-10 | アミラ ファーマシューティカルス,インコーポレーテッド | Compounds as lysophosphatidic acid receptor antagonists |
GB2474748B (en) * | 2009-10-01 | 2011-10-12 | Amira Pharmaceuticals Inc | Polycyclic compounds as lysophosphatidic acid receptor antagonists |
GB2474120B (en) | 2009-10-01 | 2011-12-21 | Amira Pharmaceuticals Inc | Compounds as Lysophosphatidic acid receptor antagonists |
AU2011338561A1 (en) | 2010-12-07 | 2013-07-25 | Amira Pharmaceuticals, Inc. | Lysophosphatidic acid receptor antagonists and their use in the treatment of fibrosis |
WO2012138797A1 (en) | 2011-04-05 | 2012-10-11 | Amira Pharmaceuticals, Inc. | 3- or 5 - bi phenyl - 4 - ylisoxazole - based compounds useful for the treatment of fibrosis, pain, cancer and respiratory, allergic, nervous system or cardiovascular disorders |
WO2013020622A1 (en) * | 2011-08-08 | 2013-02-14 | Merck Patent Gmbh | N-(benzimimdazol-2-yl)-cyclopropane carboxamides as lysophosphatidic acid antagonists |
CN104066729A (en) | 2011-08-15 | 2014-09-24 | 英特穆恩公司 | Lysophosphatidic acid receptor antagonists |
WO2013070879A1 (en) * | 2011-11-10 | 2013-05-16 | Bristol-Myers Squibb Company | Methods for treating spinal cord injury with lpa receptor antagonists |
EP2783016A1 (en) | 2011-11-22 | 2014-10-01 | Intermune, Inc. | Methods of diagnosing and treating idiopathic pulmonary fibrosis |
US9447078B2 (en) | 2012-01-20 | 2016-09-20 | Acucela Inc. | Substituted heterocyclic compounds for disease treatment |
WO2014104372A1 (en) | 2012-12-28 | 2014-07-03 | 宇部興産株式会社 | Halogen-substituted heterocyclic compound |
WO2014159814A1 (en) * | 2013-03-13 | 2014-10-02 | Patricia Oliver | Formulations and tablets for treatment or prevention of neurological disorders |
WO2014145873A2 (en) * | 2013-03-15 | 2014-09-18 | Epigen Biosciences, Inc. | Heterocyclic compounds useful in the treatment of disease |
EA038294B1 (en) * | 2013-05-24 | 2021-08-05 | Эпиджен Байосайенсиз, Инк. | Heterocyclic compounds useful in the treatment of diseases |
CN105873907B (en) | 2013-12-05 | 2019-03-12 | 拜耳作物科学股份公司 | N- naphthenic base-N- { [2- (naphthenic base that 1- replaces) phenyl] methylene }-(thio) carboxamides derivatives |
CN105793243A (en) | 2013-12-05 | 2016-07-20 | 拜耳作物科学股份公司 | N-cycloalkyl-n-{[2-(1-substitutedcycloalkyl)phenyl]methylene}-(thio)carboxamide derivatives |
AU2015229188A1 (en) | 2014-03-13 | 2016-09-29 | Proteostasis Therapeutics, Inc. | Compounds, compositions, and methods for increasing CFTR activity |
EP3116870A1 (en) | 2014-03-13 | 2017-01-18 | Proteostasis Therapeutics, Inc. | Compounds, compositions, and methods for increasing cftr activity |
EP3157917B1 (en) | 2014-06-19 | 2020-03-18 | Proteostasis Therapeutics, Inc. | Compounds, compositions and methods of increasing cftr activity |
CN106458964B (en) | 2014-06-27 | 2019-11-22 | 宇部兴产株式会社 | The salt of halogen substituted heterocyclic compound |
MA41253A (en) | 2014-12-23 | 2017-10-31 | Proteostasis Therapeutics Inc | COMPOUNDS, COMPOSITIONS AND PROCESSES TO INCREASE THE ACTIVITY OF CFTR |
WO2016105468A1 (en) | 2014-12-23 | 2016-06-30 | Proteostasis Therapeutics, Inc. | Derivatives of 3-heteroarylisoxazol-5-carboxylic amide useful for the treatment of inter alia cystic fibrosis |
CA2971855A1 (en) | 2014-12-23 | 2016-06-30 | Proteostasis Therapeutics, Inc. | Derivatives of 5-(hetero)arylpyrazol-3-carboxylic amide or 1-(hetero)aryltriazol-4-carboxylic amide useful for the treatment of inter alia cystic fibrosis |
WO2016105477A1 (en) | 2014-12-23 | 2016-06-30 | Proteostasis Therapeutics, Inc | Derivatives of 5-phenyl- or 5-heteroarylthiazol-2-carboxylic amide useful for the treatment of inter alia cystic fibrosis |
JP6929792B2 (en) | 2015-02-16 | 2021-09-01 | ザ ユニバーシティ オブ クィーンズランド | Sulfonylureas and related compounds and their use |
CA2988306A1 (en) | 2015-06-05 | 2016-12-08 | Vertex Pharmaceuticals Incorporated | Triazoles for the treatment of demyelinating diseases |
AU2016297886B2 (en) | 2015-07-24 | 2020-12-10 | Proteostasis Therapeutics, Inc. | Compounds, compositions and methods of increasing CFTR activity |
BR112018007021B1 (en) | 2015-10-06 | 2024-01-09 | Proteostasis Therapeutics, Inc | Compound, composition comprising said compounds and use thereof to treat cystic fibrosis |
MA43775A (en) | 2016-04-07 | 2021-05-05 | Proteostasis Therapeutics Inc | ANALOGUES OF IVACAFTOR CONTAINING SILICON ATOMS |
AU2017280206A1 (en) | 2016-06-21 | 2019-01-17 | Proteostasis Therapeutics, Inc. | Compounds, compositions, and methods for increasing CFTR activity |
AR108838A1 (en) | 2016-06-21 | 2018-10-03 | Bristol Myers Squibb Co | CARBAMOYLOXIMETHYL ACID TRIAZOL CYCLOHEXILO AS LPA ANTAGONISTS |
WO2018106646A1 (en) | 2016-12-06 | 2018-06-14 | Vertex Pharmaceuticals Incorporated | Aminotriazoles for the treatment of demyelinating diseases |
WO2018106641A1 (en) | 2016-12-06 | 2018-06-14 | Vertex Pharmaceuticals Incorporated | Pyrazoles for the treatment of demyelinating diseases |
WO2018106643A1 (en) | 2016-12-06 | 2018-06-14 | Vertex Pharmaceuticals Incorporated | Heterocyclic azoles for the treatment of demyelinating diseases |
US10961242B2 (en) | 2017-05-17 | 2021-03-30 | Legochem Biosciences, Inc. | Compounds as autotaxin inhibitors and pharmaceutical compositions comprising the same |
KR101798840B1 (en) | 2017-05-17 | 2017-11-17 | 주식회사 레고켐 바이오사이언스 | Novel Compounds as Autotaxin Inhibitors and Pharmaceutical Compositions Comprising the Same |
RS62910B1 (en) | 2017-07-07 | 2022-03-31 | Inflazome Ltd | Novel sulfonamide carboxamide compounds |
US11370776B2 (en) | 2017-07-07 | 2022-06-28 | Inflazome Limited | Sulfonylureas and sulfonylthioureas as NLRP3 inhibitors |
RU2020110219A (en) * | 2017-08-15 | 2021-09-17 | Инфлазоум Лимитед | SULFONYLUREAS AND SULFONYLTHIUREAS AS NLRP3 INHIBITORS |
US11542255B2 (en) | 2017-08-15 | 2023-01-03 | Inflazome Limited | Sulfonylureas and sulfonylthioureas as NLRP3 inhibitors |
US11926600B2 (en) | 2017-08-15 | 2024-03-12 | Inflazome Limited | Sulfonylureas and sulfonylthioureas as NLRP3 inhibitors |
RU2020110366A (en) * | 2017-08-15 | 2021-09-16 | Инфлазоум Лимитед | NEW COMPOUNDS OF SULFONAMIDE CARBOXAMIDES |
WO2019041340A1 (en) * | 2017-09-04 | 2019-03-07 | Eli Lilly And Company | Lysophosphatidic acid receptor 1 (lpar1) inhibitor compounds |
US11319315B2 (en) | 2017-12-19 | 2022-05-03 | Bristol-Myers Squibb Company | Cyclohexyl acid triazole azoles as LPA antagonists |
KR20200100753A (en) | 2017-12-19 | 2020-08-26 | 브리스톨-마이어스 스큅 컴퍼니 | Cyclohexyl acid pyrazole azole as an LPA antagonist |
KR20200100722A (en) | 2017-12-19 | 2020-08-26 | 브리스톨-마이어스 스큅 컴퍼니 | Cyclohexyl acid isoxazole azine as an LPA antagonist |
WO2019126087A1 (en) * | 2017-12-19 | 2019-06-27 | Bristol-Myers Squibb Company | Cyclohexyl acid isoxazole azoles as lpa antagonists |
JP7208240B2 (en) | 2017-12-19 | 2023-01-18 | ブリストル-マイヤーズ スクイブ カンパニー | Cyclohexylate triazole azines as LPA antagonists |
CN112041304A (en) | 2017-12-19 | 2020-12-04 | 百时美施贵宝公司 | Isoxazole N-linked carbamoylcyclohexanoic acids as LPA antagonists |
US11261174B2 (en) | 2017-12-19 | 2022-03-01 | Bristol-Myers Squibb Company | Pyrazole O-linked carbamoyl cyclohexyl acids as LPA antagonists |
KR20200101957A (en) | 2017-12-19 | 2020-08-28 | 브리스톨-마이어스 스큅 컴퍼니 | Isoxazole O-linked carbamoyl cyclohexyl acid as LPA antagonist |
EA202091500A1 (en) | 2017-12-19 | 2020-09-14 | Бристол-Маерс Сквибб Компани | Pyrazole N-Bonded Carbamoylcyclohexyl Acids as LPA Antagonists |
CN112189010A (en) | 2017-12-19 | 2021-01-05 | 百时美施贵宝公司 | Triazole N-linked carbamoylcyclohexanoic acids as LPA antagonists |
CN112055710A (en) | 2017-12-19 | 2020-12-08 | 百时美施贵宝公司 | Cyclohexyl acid pyrazole azines as LPA antagonists |
US11905252B2 (en) | 2018-03-02 | 2024-02-20 | Inflazome Limited | Compounds |
CA3046894A1 (en) * | 2018-06-18 | 2019-12-18 | Epigen Biosciences, Inc. | Heterocyclic compounds useful in the treatment of disease |
MX2022001264A (en) * | 2019-07-30 | 2022-02-22 | Taisho Pharmaceutical Co Ltd | Urea compound for antagonizing lpa1 receptor. |
CA3158743A1 (en) | 2019-11-15 | 2021-05-20 | Gilead Sciences, Inc. | Triazole carbamate pyridyl sulfonamides as lpa receptor antagonists and uses thereof |
TW202134213A (en) * | 2019-11-29 | 2021-09-16 | 日商小野藥品工業股份有限公司 | Compound having lysophosphatidic acid receptor agonistic activity and pharmaceutical use of said compound |
US11702407B2 (en) | 2020-06-03 | 2023-07-18 | Gilead Sciences, Inc. | LPA receptor antagonists and uses thereof |
TW202344504A (en) | 2020-06-03 | 2023-11-16 | 美商基利科學股份有限公司 | Lpa receptor antagonists and uses thereof |
US11939318B2 (en) | 2021-12-08 | 2024-03-26 | Gilead Sciences, Inc. | LPA receptor antagonists and uses thereof |
TW202342017A (en) | 2022-02-25 | 2023-11-01 | 美商洛子峰生物有限公司 | Compounds and compositions for treating conditions associated with lpa receptor activity |
CN114907282B (en) * | 2022-05-24 | 2023-08-22 | 华南理工大学 | Method for synthesizing 4-phenyl alkenyl isoxazole derivative |
CN117126044B (en) * | 2023-04-12 | 2024-01-26 | 延边大学 | Microwave-assisted synthesis method of methyl ketone compound |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20030114505A1 (en) * | 2000-02-18 | 2003-06-19 | Akihiro Ueno | Novel isoxazole and thiazole compounds and use thereof as drugs |
EP1340749A1 (en) * | 2000-11-17 | 2003-09-03 | Takeda Chemical Industries, Ltd. | Isoxazole derivatives |
JP2003261545A (en) * | 2001-12-28 | 2003-09-19 | Takeda Chem Ind Ltd | Neurotrophic factor production/secretion accelerator |
Family Cites Families (77)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4229447A (en) | 1979-06-04 | 1980-10-21 | American Home Products Corporation | Intraoral methods of using benzodiazepines |
US4476116A (en) | 1982-12-10 | 1984-10-09 | Syntex (U.S.A.) Inc. | Polypeptides/chelating agent nasal compositions having enhanced peptide absorption |
US5116817A (en) | 1982-12-10 | 1992-05-26 | Syntex (U.S.A.) Inc. | LHRH preparations for intranasal administration |
US4596795A (en) | 1984-04-25 | 1986-06-24 | The United States Of America As Represented By The Secretary, Dept. Of Health & Human Services | Administration of sex hormones in the form of hydrophilic cyclodextrin derivatives |
DE3684446D1 (en) | 1985-12-28 | 1992-04-23 | Sumitomo Pharma | MEDICINAL PRODUCTS WITH DELAYED RELEASED RELEASE. |
US4755386A (en) | 1986-01-22 | 1988-07-05 | Schering Corporation | Buccal formulation |
JP2633641B2 (en) | 1988-08-26 | 1997-07-23 | 本田技研工業株式会社 | Exhaust gas concentration detector |
US5739136A (en) | 1989-10-17 | 1998-04-14 | Ellinwood, Jr.; Everett H. | Intraoral dosing method of administering medicaments |
US5017381A (en) | 1990-05-02 | 1991-05-21 | Alza Corporation | Multi-unit pulsatile delivery system |
US5229135A (en) | 1991-11-22 | 1993-07-20 | Prographarm Laboratories | Sustained release diltiazem formulation |
US5612359A (en) | 1994-08-26 | 1997-03-18 | Bristol-Myers Squibb Company | Substituted biphenyl isoxazole sulfonamides |
JPH096712A (en) | 1995-06-23 | 1997-01-10 | Canon Inc | Data processor |
GB9523946D0 (en) | 1995-11-23 | 1996-01-24 | Bayer Ag | Leukotriene antagonistic benzoic acid derivatives |
US5837284A (en) | 1995-12-04 | 1998-11-17 | Mehta; Atul M. | Delivery of multiple doses of medications |
ATE236890T1 (en) | 1996-12-23 | 2003-04-15 | Bristol Myers Squibb Pharma Co | OXYGEN OR SULFUR CONTAINING 5-MEMBED HETEROAROMATIC DERIVATIVES AS FACTOR XA INHIBITORS |
JP3237608B2 (en) | 1997-04-21 | 2001-12-10 | 住友製薬株式会社 | Isoxazole derivative |
US5840329A (en) | 1997-05-15 | 1998-11-24 | Bioadvances Llc | Pulsatile drug delivery system |
US6391452B1 (en) | 1997-07-18 | 2002-05-21 | Bayer Corporation | Compositions for nasal drug delivery, methods of making same, and methods of removing residual solvent from pharmaceutical preparations |
CA2368630A1 (en) | 1999-04-02 | 2000-10-12 | Ruth R. Wexler | Aryl sulfonyls as factor xa inhibitors |
DE10013485C1 (en) | 2000-03-18 | 2001-07-12 | Krupp Bilstein Gmbh | Vehicle lifting jack has cog segment of pivoted carrier arm cooperating with cog section of control slider displaced parallel to support column |
JPWO2001072723A1 (en) | 2000-03-28 | 2004-01-08 | 日本曹達株式会社 | Oxa (thia) zolidine derivatives and anti-inflammatory drugs |
WO2002000651A2 (en) | 2000-06-27 | 2002-01-03 | Bristol-Myers Squibb Pharma Company | Factor xa inhibitors |
DE60234318D1 (en) | 2001-02-08 | 2009-12-24 | Ono Pharmaceutical Co | FOR THE TREATMENT OF RESPIRATORY DISEASES, COMPRISING MEANS FOR THE CONTROL OF THE LPA RECEPTOR |
US7521192B2 (en) | 2001-04-18 | 2009-04-21 | Rigel Pharmaceuticals, Inc. | EDG: modulators of lymphocyte activation and migration |
ES2312588T3 (en) | 2001-07-17 | 2009-03-01 | Ono Pharmaceutical Co., Ltd. | REGULATION OF THE PANCREATIC JUICE SECRETION UNDERSTANDING A LPA RECEIVER REGULATION AGENT. |
MY151199A (en) | 2001-11-02 | 2014-04-30 | Rigel Pharmaceuticals Inc | Substituted diphenyl heterocycles useful for treating hcv infection |
JP4569106B2 (en) | 2001-12-25 | 2010-10-27 | 味の素株式会社 | Organ fibrosis inhibitor |
EP1513522A2 (en) | 2002-01-18 | 2005-03-16 | Sri International | Methods of treating conditions associated with an edg receptor |
US20050101518A1 (en) | 2002-01-18 | 2005-05-12 | David Solow-Cordero | Methods of treating conditions associated with an EDG-2 receptor |
US20050113283A1 (en) | 2002-01-18 | 2005-05-26 | David Solow-Cordero | Methods of treating conditions associated with an EDG-4 receptor |
US20050261298A1 (en) | 2002-01-18 | 2005-11-24 | David Solow-Cordero | Methods of treating conditions associated with an Edg-7 receptor |
JP4547912B2 (en) | 2002-03-05 | 2010-09-22 | 小野薬品工業株式会社 | 8-Azaprostaglandin derivative compound and drug containing the compound as an active ingredient |
WO2003094965A2 (en) | 2002-05-08 | 2003-11-20 | Neuronova Ab | Modulation of neural stem cells with s1p or lpa receptor agonists |
JP2005529923A (en) | 2002-05-13 | 2005-10-06 | イーライ・リリー・アンド・カンパニー | Polycyclic compounds for use as melanin-concentrating hormone antagonists in the treatment of obesity and diabetes |
AU2003241833A1 (en) | 2002-05-28 | 2003-12-12 | Ono Pharmaceutical Co., Ltd. | Beta-ALANINE DERIVATIVE AND USE THEREOF |
EP1550461A1 (en) | 2002-06-26 | 2005-07-06 | Ono Pharmaceutical Co., Ltd. | Remedy for chronic disease |
JP4691988B2 (en) | 2002-10-03 | 2011-06-01 | 小野薬品工業株式会社 | LPA receptor antagonist |
PL376971A1 (en) | 2002-11-19 | 2006-01-23 | Amgen, Inc. | Amplified genes involved in cancer |
US20040192739A1 (en) | 2003-01-16 | 2004-09-30 | David Solow-Cordero | Methods of treating conditions associated with an Edg-2 receptor |
US20050065194A1 (en) | 2003-01-16 | 2005-03-24 | Geetha Shankar | Methods of treating conditions associated with an Edg-2 receptor |
US20040167132A1 (en) | 2003-01-16 | 2004-08-26 | Geetha Shankar | Methods of treating conditions associted with an Edg-2 receptor |
US7135469B2 (en) | 2003-03-18 | 2006-11-14 | Bristol Myers Squibb, Co. | Linear chain substituted monocyclic and bicyclic derivatives as factor Xa inhibitors |
US20060089398A1 (en) * | 2003-03-19 | 2006-04-27 | Gang Liu | Isoxazole carboxamide derivatives as ghrelin receptor modulators |
US7115642B2 (en) | 2003-05-02 | 2006-10-03 | Rigel Pharmaceuticals, Inc. | Substituted diphenyl isoxazoles, pyrazoles and oxadiazoles useful for treating HCV infection |
PL1638551T3 (en) | 2003-05-19 | 2012-05-31 | Irm Llc | Immunosuppressant compounds and compositions |
WO2005012269A1 (en) | 2003-08-05 | 2005-02-10 | Ajinomoto Co., Inc. | Novel azole compound |
ATE528276T1 (en) | 2003-12-19 | 2011-10-15 | Ono Pharmaceutical Co | LYSOPHOSPHATIDYL ACID RECEPTOR ANTAGONIST COMPOUNDS AND THEIR APPLICATIONS |
DE10360369A1 (en) | 2003-12-22 | 2005-07-14 | Bayer Cropscience Ag | amides |
WO2005123671A1 (en) | 2004-06-22 | 2005-12-29 | Taisho Pharmaceutical Co., Ltd. | Pyrrole derivative |
US7405237B2 (en) * | 2004-07-28 | 2008-07-29 | Celgene Corporation | Isoindoline compounds and methods of their use |
JP2006096712A (en) | 2004-09-30 | 2006-04-13 | Senju Pharmaceut Co Ltd | Corneal sensitivity improver containing lpa receptor antagonist |
AR055041A1 (en) | 2005-03-23 | 2007-08-01 | Merck Frosst Canada Ltd | TIADIAZOLS AND OXADIAZOLS AS INHIBITORS OF THE SYNTHESIS OF LEUCOTRIENOS. PHARMACEUTICAL COMPOSITIONS. |
WO2006131336A1 (en) | 2005-06-08 | 2006-12-14 | Novartis Ag | POLYCYCLIC OXADIAZOLES OR I SOXAZOLES AND THEIR USE AS SlP RECEPTOR LIGANDS |
WO2007007588A1 (en) | 2005-07-08 | 2007-01-18 | Ono Pharmaceutical Co., Ltd. | Compound having cyclic group with planarity as core |
AU2006279211A1 (en) | 2005-08-11 | 2007-02-15 | Merck Frosst Canada Ltd | Novel substituted 1,2,3-triazolylmethyl-benzothiophene or -indole and their use as leukotriene biosynthesis inhibitors |
JP2009506046A (en) | 2005-08-23 | 2009-02-12 | アイアールエム・リミテッド・ライアビリティ・カンパニー | Immunosuppressant compounds and compositions |
US7405302B2 (en) | 2005-10-11 | 2008-07-29 | Amira Pharmaceuticals, Inc. | 5-lipoxygenase-activating protein (FLAP) inhibitors |
US20070219206A1 (en) | 2005-11-04 | 2007-09-20 | Amira Pharmaceuticals, Inc. | 5-lipoxygenase-activating protein (flap) inhibitors |
US7977359B2 (en) | 2005-11-04 | 2011-07-12 | Amira Pharmaceuticals, Inc. | 5-lipdxygenase-activating protein (FLAP) inhibitors |
US20070225285A1 (en) | 2005-11-04 | 2007-09-27 | Amira Pharmaceuticals, Inc. | 5-lipoxygenase-activating protein (flap) inhibitors |
CA2636043A1 (en) | 2006-01-23 | 2007-08-02 | Amira Pharmaceuticals, Inc. | Tricyclic inhibitors of 5-lipoxygenase |
CA2643670A1 (en) | 2006-02-27 | 2007-08-30 | Sterix Limited | Diaryl compounds as non-steroidal inhibitors of 17-beta hydroxysteroid dehydrogenase and/or steroid sulphatase for the treatment of oestrogen-related diseases such as hormone dependent breast cancer |
US20090029949A1 (en) | 2006-05-25 | 2009-01-29 | Parrill-Baker Abby L | GPCR Ligands Identified by Computational Modeling |
WO2008024979A2 (en) | 2006-08-24 | 2008-02-28 | The Scripps Research Institute | Methods utilizing cell-signaling lysophospholipids |
US20080051372A1 (en) | 2006-08-24 | 2008-02-28 | The Scripps Research Institute | Methods utilizing cell-signaling lysophospholipids |
WO2008112201A2 (en) | 2007-03-12 | 2008-09-18 | The General Hospital Corporation | Lysophosphatidic acid receptor targeting for lung disease |
US9163091B2 (en) | 2007-05-30 | 2015-10-20 | Lpath, Inc. | Compositions and methods for binding lysophosphatidic acid |
US20090069288A1 (en) | 2007-07-16 | 2009-03-12 | Breinlinger Eric C | Novel therapeutic compounds |
SI2303270T1 (en) | 2008-05-05 | 2018-01-31 | Sanofi | Acylamino-substituted fused cyclopentanecarboxylic acid derivatives and their use as pharmaceuticals |
JP4933512B2 (en) | 2008-10-09 | 2012-05-16 | 住友化学株式会社 | Light guide plate |
US8455499B2 (en) | 2008-12-11 | 2013-06-04 | Amira Pharmaceuticals, Inc. | Alkyne antagonists of lysophosphatidic acid receptors |
GB2466121B (en) | 2008-12-15 | 2010-12-08 | Amira Pharmaceuticals Inc | Antagonists of lysophosphatidic acid receptors |
GB2470833B (en) | 2009-06-03 | 2011-06-01 | Amira Pharmaceuticals Inc | Polycyclic antagonists of lysophosphatidic acid receptors |
JP2013501064A (en) | 2009-08-04 | 2013-01-10 | アミラ ファーマシューティカルス,インコーポレーテッド | Compounds as lysophosphatidic acid receptor antagonists |
GB2474120B (en) | 2009-10-01 | 2011-12-21 | Amira Pharmaceuticals Inc | Compounds as Lysophosphatidic acid receptor antagonists |
WO2011041551A1 (en) * | 2009-10-01 | 2011-04-07 | Intermune, Inc. | Therapeutic antiviral peptides |
GB2474748B (en) * | 2009-10-01 | 2011-10-12 | Amira Pharmaceuticals Inc | Polycyclic compounds as lysophosphatidic acid receptor antagonists |
-
2010
- 2010-09-28 GB GB1016314.5A patent/GB2474120B/en not_active Expired - Fee Related
- 2010-10-01 TW TW099133646A patent/TWI401082B/en not_active IP Right Cessation
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- 2010-10-01 EP EP10821369A patent/EP2483253A4/en not_active Withdrawn
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- 2010-10-01 WO PCT/US2010/051199 patent/WO2011041729A2/en active Application Filing
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- 2010-10-01 IN IN2177DEN2012 patent/IN2012DN02177A/en unknown
- 2010-10-01 IN IN2735DEN2012 patent/IN2012DN02735A/en unknown
- 2010-10-01 US US12/896,080 patent/US8217066B2/en active Active
- 2010-10-01 US US13/498,491 patent/US9090573B2/en active Active
- 2010-10-01 UY UY0001032926A patent/UY32926A/en not_active Application Discontinuation
- 2010-10-01 JP JP2012532368A patent/JP2013506695A/en active Pending
- 2010-10-01 CN CN2010800546595A patent/CN102639515A/en active Pending
-
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- 2015-06-30 US US14/755,383 patent/US9624182B2/en active Active
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20030114505A1 (en) * | 2000-02-18 | 2003-06-19 | Akihiro Ueno | Novel isoxazole and thiazole compounds and use thereof as drugs |
EP1340749A1 (en) * | 2000-11-17 | 2003-09-03 | Takeda Chemical Industries, Ltd. | Isoxazole derivatives |
JP2003261545A (en) * | 2001-12-28 | 2003-09-19 | Takeda Chem Ind Ltd | Neurotrophic factor production/secretion accelerator |
Non-Patent Citations (2)
Title |
---|
MASAHIKO KAINUMA ET AL: "Design, synthesis, and evaluation of non-steroidal farnesoid X receptor (FXR) antagonist", BIOORGANIC & MEDICINAL CHEMISTRY, vol. 15, no. 7, 2007, pages 2587 - 2600, XP005922449 * |
See also references of EP2483253A4 * |
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EP2483252B1 (en) | 2017-03-08 |
JP2013506695A (en) | 2013-02-28 |
EP2483252A2 (en) | 2012-08-08 |
WO2011041694A2 (en) | 2011-04-07 |
CN102666504A (en) | 2012-09-12 |
WO2011041694A3 (en) | 2011-08-18 |
CN102666504B (en) | 2016-06-01 |
US20120289522A1 (en) | 2012-11-15 |
IN2012DN02735A (en) | 2015-09-11 |
US8217066B2 (en) | 2012-07-10 |
EP2483253A4 (en) | 2013-04-03 |
GB2474120B (en) | 2011-12-21 |
GB2474120A (en) | 2011-04-06 |
GB201016314D0 (en) | 2010-11-10 |
EP2483253A2 (en) | 2012-08-08 |
JP2013506694A (en) | 2013-02-28 |
AR078497A1 (en) | 2011-11-09 |
US20110082181A1 (en) | 2011-04-07 |
US9624182B2 (en) | 2017-04-18 |
TW201116278A (en) | 2011-05-16 |
US20150329502A1 (en) | 2015-11-19 |
EP2483252A4 (en) | 2013-04-03 |
IN2012DN02177A (en) | 2015-08-21 |
WO2011041729A2 (en) | 2011-04-07 |
US9090573B2 (en) | 2015-07-28 |
CN102639515A (en) | 2012-08-15 |
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